Canonical Allele Identifier: CA1584260173

Gene: TXNDC15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893476G= , CM000667.2:g.134893476G=	GRCh38
NC_000005.9:g.134229166G= , CM000667.1:g.134229166G=	GRCh37
NC_000005.8:g.134257065G=	NCBI36
NG_053174.1:g.24707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-16G= MANE Select	ENSP00000351157.5:n.592-16G=
ENST00000358387.8:c.592-16G=	ENSP00000351157.4:n.592-16G=
ENST00000505174.1:n.1299G=
ENST00000506350.1:n.31-16G=
ENST00000507024.5:c.*410-16G=	ENSP00000424716.1:n.*410-16G=
ENST00000508779.1:c.543-16G=
ENST00000511070.5:c.104-16G=	ENSP00000423609.1:n.104-16G=
NM_024715.3:c.592-16G=	NP_078991.3:n.592-16G=
NM_001350735.1:c.388-16G=	NP_001337664.1:n.388-16G=
NM_024715.4:c.592-16G= MANE Select	NP_078991.3:n.592-16G=
NM_001350735.2:c.388-16G=	NP_001337664.1:n.388-16G=